{{Rsnum
|rsid=104894100
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AGPAT2
|position=136673906
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGPAT2
}}{{omim
|id=603100
|rsnum=104894100
|variant=0004
}}{{ClinVar
|rsid=104894100
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=139568358
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=AGPAT2:10555
|GENE_NAME=AGPAT2
|GENE_ID=10555
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.139568358A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603100.0004
|CLNSIG=5
|CLNCUI=C1720862
|CLNDBN=Congenital generalized lipodystrophy type 1
|Disease=Congenital generalized lipodystrophy type 1
|CLNACC=RCV000007006.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1212:C1720862:608594:528
}}